Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1569354918 1.000 0.120 X 134473357 splice acceptor variant A/T snv 1
rs137852499 1.000 0.120 X 134473377 missense variant G/A snv 1
rs1135401801 1.000 0.120 X 134473378 missense variant G/T snv 1
rs137852480 1.000 0.120 X 134473453 missense variant T/C snv 1
rs137852491 1.000 0.120 X 134473465 missense variant G/A snv 4.4E-05 1
rs387906725 0.882 0.160 X 134475189 missense variant G/A snv 3
rs1556026984 0.925 0.120 X 134475194 missense variant G/C snv 4
rs137852494 0.925 0.160 X 134475197 stop gained C/G;T snv 2
rs137852502 1.000 0.120 X 134475201 missense variant A/G snv 1
rs137852495 0.925 0.120 X 134475216 missense variant T/C snv 2
rs137852500 1.000 0.120 X 134475218 missense variant G/A snv 1
rs1228634091 1.000 0.120 X 134475225 missense variant A/G snv 1.1E-05 1
rs137852506 1.000 0.120 X 134475239 missense variant C/T snv 1
rs137852487 1.000 0.120 X 134475255 missense variant G/A snv 1
rs137852488 1.000 0.120 X 134475257 missense variant G/C snv 1
rs137852481 1.000 0.120 X 134475268 missense variant C/A snv 1
rs137852501 1.000 0.120 X 134475278 missense variant C/G snv 1
rs137852478 1.000 0.120 X 134475285 missense variant A/T snv 1
rs137852485 0.925 0.120 X 134475358 missense variant C/A snv 2
rs137852489 0.925 0.160 X 134486471 stop gained C/A;T snv 2.4E-05 2
rs137852482 1.000 0.120 X 134486475 missense variant C/T snv 1
rs369065223 0.925 0.160 X 134486514 stop gained C/G;T snv 5.5E-06 2
rs137852483 1.000 0.120 X 134490192 missense variant T/A snv 1
rs137852477 1.000 0.120 X 134490199 missense variant T/G snv 1
rs137852503 1.000 0.120 X 134493524 missense variant G/A snv 1